Evaluating apheresis platelets at reduced dose as a contingency measure for extreme shortages

被引:5
作者
Smethurst, Peter A. [1 ]
McAndrew, Margaret [1 ]
Proffitt, Susan [1 ]
Procter, Simon [2 ]
Davies, Jane [3 ]
New, Helen, V [4 ,5 ]
Stanworth, Simon J. [5 ,6 ,7 ,8 ]
Doughty, Heidi [5 ]
Cardigan, Rebecca [1 ,9 ]
机构
[1] NHS Blood & Transplant, Component Dev Lab, Long Rd, Cambridge CB2 0PT, England
[2] Qual Monitoring NHS Blood & Transplant, London, England
[3] Tech & Amp Sci Dev NHS Blood & Transplant, London, England
[4] Imperial Coll London, Ctr Haematol, London, England
[5] NHS Blood & Transplant, Clin Serv Directorate, London, England
[6] Univ Oxford, Radcliffe Dept Med, Oxford, England
[7] NIHR Oxford Biomed Res Ctr, Oxford, England
[8] Oxford Univ Hosp NHS Fdn Trust, Dept Haematol, Oxford, England
[9] Univ Cambridge, Dept Haematol, Cambridge, England
关键词
dose; platelets; storage lesion; P-SELECTIN; TRANSFUSION; STORAGE; QUALITY; BLOOD;
D O I
10.1111/trf.16723
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The COVID19 pandemic highlights the need for contingency planning in the event of blood shortages. To increase platelet supply, we assessed the operational impact and effect on platelet quality of splitting units prior to storage. Study design and methods: Using production figures, we modeled the impact on unit numbers, platelet counts, and volumes of splitting only apheresis double donations into three units (yielding 2/3 doses), or all standard dose units in half. To assess quality, eight pools of three ABO/Rh-matched apheresis (Trima Accel) double donations in plasma were split to 2/3 and 1/2 volumes in both Terumo and Fresenius storage bags. These were irradiated and subject to maximal permitted periods of nonagitation (3 x 8 h) before comparing platelet quality markers (including pH, CD62P expression) to Day 9 of storage. Results: Splitting all double donations into three predicted inventory expansion of 23% overall whereas halving all standard dose units clearly doubles stock. In our study, 2/3 and 1/2 doses contained 153 +/- 15 x 10(9) (similar to 138 ml) and 113 +/- 11 x 10(9) (similar to 102 ml) platelets respectively. Following storage, higher pH was observed in 2/3 than in 1/2 doses and in Terumo compared to Fresenius bags. The higher pH was reflected in better quality markers, including lower CD62P expression. Despite the differences, on Day 8 (of pH monitoring at expiry) all 2/3 doses and most 1/2 doses were >= 6.4. Conclusion: A strategy to split apheresis platelets in plasma to lower doses is feasible, maintains acceptable platelet quality, and should be considered by blood services in response to extreme shortages.
引用
收藏
页码:173 / 182
页数:10
相关论文
共 30 条
[1]  
Association for the Advancement of Blood & Biotherapies (AABB), 2020, Standards for Blood Banks and Transfusion Services, V32nd
[2]   Platelet transfusion versus standard care after acute stroke due to spontaneous cerebral haemorrhage associated with antiplatelet therapy (PATCH): a randomised, open-label, phase 3 trial [J].
Baharoglu, M. Irem ;
Cordonnier, Charlotte ;
Salman, Rustam Al-Shahi ;
de Gans, Koen ;
Koopman, Maria M. ;
Brand, Anneke ;
Majoie, Charles B. ;
Beenen, Ludo F. ;
Marquering, Henk A. ;
Vermeulen, Marinus ;
Nederkoorn, Paul J. ;
de Haan, Rob J. ;
Roos, Yvo B. .
LANCET, 2016, 387 (10038) :2605-2613
[3]   The argument(s) for lowering the US minimum required content of apheresis platelet components [J].
Benjamin, Richard J. ;
Katz, Louis ;
Gammon, Richard R. ;
Stramer, Susan L. ;
Quinley, Eva ;
Armitage, John ;
Barnes, Linda ;
Benjamin, Richard J. ;
Boraz, Margie ;
Borge, P. Dayand ;
Bracey, Art ;
Cohn, Claudia S. ;
Crawford, Chris ;
Evans, Jill ;
Gammon, Richard ;
Hoiles, Jonathan ;
Katz, Lou ;
Koski, Karen ;
Menitove, Jay ;
Quinley, Eva ;
Schiffer, Charles A. ;
Stramer, Susan ;
Strauss, Donna ;
Stubbs, James R. ;
Waller, Ned ;
Rowe, Kathleen .
TRANSFUSION, 2019, 59 (02) :779-788
[4]   Randomized Trial of Platelet-Transfusion Thresholds in Neonates [J].
Curley, Anna ;
Stanworth, Simon J. ;
Willoughby, Karen ;
Fustolo-Gunnink, Susanna F. ;
Venkatesh, Vidheya ;
Hudson, Cara ;
Deary, Alison ;
Hodge, Renate ;
Hopkins, Valerie ;
Santamaria, Beatriz Lopez ;
Mora, Ana ;
Llewelyn, Charlotte ;
D'Amore, Angela ;
Khan, Rizwan ;
Onland, Wes ;
Lopriore, Enrico ;
Fijnvandraat, Karin ;
New, Helen ;
Clarke, Paul ;
Watts, Timothy .
NEW ENGLAND JOURNAL OF MEDICINE, 2019, 380 (03) :242-251
[5]   In vitro pH effects on in vivo recovery and survival of platelets: an analysis by the BEST Collaborative [J].
Dumont, Larry J. ;
AuBuchon, James P. ;
Gulliksson, Hans ;
Slichter, Sherrill J. ;
Elfath, M. Dean ;
Holme, Stein ;
Murphy, James R. ;
Rose, Leslie E. ;
Popovsky, Mark A. ;
Murphy, Scott .
TRANSFUSION, 2006, 46 (08) :1300-1305
[6]  
EQDM, 2020, GUIDE PREPARATION US
[7]   Guidelines for the use of platelet transfusions [J].
Estcourt, Lise J. ;
Birchall, Janet ;
Allard, Shubha ;
Bassey, Stephen J. ;
Hersey, Peter ;
Kerr, Jonathan Paul ;
Mumford, Andrew D. ;
Stanworth, Simon J. ;
Tinegate, Hazel .
BRITISH JOURNAL OF HAEMATOLOGY, 2017, 176 (03) :365-394
[8]  
Galloway-Haskins R, 2013, TRANSFUSION, V53, p38A
[9]   Single platelets seal neutrophil-induced vascular breaches via GPVI during immune-complex-mediated inflammation in mice [J].
Gros, Angele ;
Syvannarath, Varouna ;
Lamrani, Lamia ;
Ollivier, Veronique ;
Loyau, Stephane ;
Goerge, Tobias ;
Nieswandt, Bernhard ;
Jandrot-Perrus, Martine ;
Ho-Tin-Noe, Benoit .
BLOOD, 2015, 126 (08) :1017-1026
[10]   How platelets safeguard vascular integrity [J].
Ho-Tin-Noe, B. ;
Demers, M. ;
Wagner, D. D. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2011, 9 :56-65